Forms and Documents
Test Details
Expand Genes
ATL1, DNMT1, IKBKAP, KIF1A, NGF, NTRK1, PRDM12, RAB7A, RETREG1, SCN11A, SCN9A, SPTLC1, SPTLC2, WNK1
- Congenital Insensitivity to Pain with Anhidrosis
- Episodic Pain Syndrome Type 3
- Hereditary Sensory and Autonomic Neuropathy (HSAN)
- Hereditary Sensory and Autonomic Neuropathy I (HSAN I)
- Hereditary Sensory and Autonomic Neuropathy II (HSAN II)
- Hereditary Sensory and Autonomic Neuropathy III (HSAN III)
- Hereditary Sensory and Autonomic Neuropathy IV (HSAN IV)
- Hereditary Sensory and Autonomic Neuropathy V (HSAN V)
- Hereditary Sensory and Autonomic Neuropathy VIII (HSAN VIII)
- Inherited Erythromelalgia (IEM)
- Paroxysmal Extreme Pain Disorder (PEPD)
- Riley Day Syndrome
- Small Fiber Neuropathy (SFN)
- Molecular confirmation of a clinical diagnosis
- To assist with decisions about treatment and management of individuals with neuropathy
- Testing of at-risk relatives for specific mutation(s) previously identified in an affected family member
- Prenatal diagnosis for known familial mutation(s) in at-risk pregnancies
Ordering
T399
4 weeks
2-5 mL Blood - Lavender Top Tube
Buccal Swabs
*Reporting times are typical, but could be extended in situations outside GeneDx's reasonable control.
Billing
81448x1
No
Yes
For price inquiries please email zebras@genedx.com
**The CPT codes provided are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.
**The CPT codes provided are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.